Department of Chemistry, Himachal Pradesh University, Shimla-171005, India.
Department of Chemistry, Himachal Pradesh University, Shimla-171005, India.
Int J Biol Macromol. 2024 Apr;264(Pt 2):130814. doi: 10.1016/j.ijbiomac.2024.130814. Epub 2024 Mar 11.
Recently, various advancements have been made in the development of functional polymeric materials for innovative applications. Herein this work, functionalization of sterculia gum (SG) was carried out via grafting of poly(2-(methacryloyloxy) ethyltrimethylammonium chloride) (METAC)-polyvinyl pyrrolidone (PVP) to develop hydrogel dressings as a platform for use in drug delivery (DD). The innovation of the present work is the exploration of inherent antioxidant and antimicrobial properties of the SG along with antimicrobial characteristic of poly(METAC) and PVP, to design the doxycycline encapsulated hydrogel dressings for better wound healing. FESEM, EDS and AFM analyzed the surface morphology of hydrogels. FTIR, C NMR and XRD inferred inclusion of poly(METAC)-PVP into polymers. C NMR confirmed the incorporation of poly(METAC) and PVP onto gum by the presence of a peak at 54.74 ppm because of methyl carbon attached to quaternary nitrogen of poly(METAC) and at 45.48 ppm due to the ring carbon of PVP along with FTIR peak at 949 cm because of CN bending of quaternary nitrogen of poy (METAC). Thermal characterization of copolymers has been performed using TGA analysis. One gram of copolymeric hydrogel dressing absorbed 6.51 ± 0.03 g simulated salivary fluid (SSF) and 7.65 ± 0.03 g simulated wound fluid (SWF). Release of doxycycline drug occurred in a sustained manner and followed the Non-Fickian diffusion mechanism from hydrogels. The release profile was most effectively described by Hixon-Crowell kinetic model. Hydrogel demonstrated biocompatibility and expressed thrombogenicity 79.7 ± 4.9 % during its polymer-blood interactions. Copolymer revealed mucoadhesive property, requiring a force of 77.00 ± 0.01 mN to detach from bio-membrane. Additionally, it exhibited antioxidant features, showing 43.81 ± 0.286 % free radical scavenging. Hydrogel dressings were mechanically stable and revealed 0.76 ± 0.09 N mm tensile strength and 9.18 ± 0.01 N burst strength. Polymer films were permeable to oxygen and water vapor and were impermeable to microorganisms. Hydrogel dressings exhibited antimicrobial properties against Pseudomonas aeruginosa and Staphylococcus aureus bacteria. Overall, these properties displayed the suitability of hydrogels for wound dressing (WD) applications which may actively enhance wound healing.
最近,在开发用于创新应用的功能性聚合物材料方面取得了各种进展。在此项工作中,通过接枝聚(2-(甲基丙烯酰氧基)乙基三甲基氯化铵)(METAC)-聚乙烯吡咯烷酮(PVP)对麻疯树胶(SG)进行了功能化,以开发水凝胶敷料作为药物输送(DD)的平台。本工作的创新之处在于探索 SG 的固有抗氧化和抗菌特性以及聚(METAC)和 PVP 的抗菌特性,以设计包封有强力霉素的水凝胶敷料以促进伤口愈合。FESEM、EDS 和 AFM 分析了水凝胶的表面形态。FTIR、C NMR 和 XRD 推断聚合物中包含聚(METAC)-PVP。C NMR 通过在 54.74 ppm 处存在归因于聚(METAC)中季氮上连接的甲基碳和在 45.48 ppm 处归因于 PVP 的环碳的峰,以及在 949 cm 处归因于聚(METAC)的季氮的 CN 弯曲的 FTIR 峰,确认了聚(METAC)和 PVP 掺入到胶中。使用 TGA 分析对共聚物的热特性进行了研究。一克共聚物水凝胶敷料吸收了 6.51±0.03g 模拟唾液(SSF)和 7.65±0.03g 模拟伤口液(SWF)。强力霉素药物的释放以持续的方式发生,并遵循水凝胶的非 Fickian 扩散机制。释放曲线最有效地由 Hixon-Crowell 动力学模型描述。水凝胶在聚合物与血液相互作用期间表现出生物相容性,血栓形成率为 79.7±4.9%。共聚物具有粘膜粘附性,从生物膜上分离需要 77.00±0.01mN 的力。此外,它还表现出抗氧化特性,显示出 43.81±0.286%的自由基清除率。水凝胶敷料具有机械稳定性,显示出 0.76±0.09Nmm 的拉伸强度和 9.18±0.01N 的破裂强度。聚合物薄膜对氧气和水蒸气具有渗透性,对微生物具有不可渗透性。水凝胶敷料对铜绿假单胞菌和金黄色葡萄球菌具有抗菌性能。总的来说,这些特性显示出水凝胶适用于伤口敷料(WD)应用,可积极促进伤口愈合。